Genetic Testing Records

Store and organize your genetic test results, DNA analysis, hereditary screening reports, and family health history in one secure digital health platform. Access your genomic information anytime and share critical insights with healthcare providers.

Genetic testing dashboard showing test results, genetic markers, and variant tracking

Store Test Details
All Test Types

Summarize Findings
Track Key Insights

Easily Share
Provider Access
CareClinic › Personal Health Records (PHR) › Genetic Test Records

Complete Genetic Data Management

Organize genetic testing results from whole genome sequencing to pharmacogenomic profiles. Track genetic variants, hereditary conditions, and personalized health recommendations in one centralized, secure location.

MULTIPLE TEST TYPE SUPPORT+

Store results from whole genome sequencing, exome sequencing, carrier screening, pharmacogenomic panels, ancestry tests, and nutrigenomic profiles. Upload PDF reports from any laboratory or manually enter genetic variants.

GENETIC VARIANT TRACKING+

Document specific SNPs, gene mutations, copy number variations, and chromosomal abnormalities. Track clinical significance, population frequency, and associated health conditions for each variant.

HEREDITARY RISK ASSESSMENT+

View genetic predispositions for cancer, cardiovascular disease, diabetes, and other conditions. Track polygenic risk scores and compare your risk to population averages with clear visualizations.

Add genetic test screen with options for whole genome sequencing, pharmacogenomics, and carrier screening tests
23andMe Panel test results showing no pathogenic variants detected with blood sample and provider details

Drug Response Data

Store medication metabolism information and track how genetic variants affect drug effectiveness.

Family Health History

Document genetic test results for family members to track inherited conditions and hereditary patterns.

Health Insights

Receive personalized recommendations based on your genetic predispositions and variants.

Raw Data Import

Import raw genetic data files from 23andMe, AncestryDNA, and other consumer testing services.

Store, Organize, and Share Your Genetic Testing Data

Upload test results from any laboratory, track genetic variants and conclusions, then securely share insights with your healthcare team for personalized care decisions.

Upload Test Results

Import genetic test reports from any laboratory or add specific variants and markers manually for comprehensive tracking.

Select genetic test type screen showing options like Amniocentesis, ACGH, Autosomal DNA, Biochemical Genetics, Carrier Screening

Review Test Conclusions

Store genetic test results with findings, variant details, and clinical interpretations for future reference and medical decisions.

Genetic test detail showing sample type, provider, date, conclusion findings, and additional clinical notes

Share with Care Team

Quickly share genetic test results with doctors, genetic counselors, or family members using secure sharing options.

Share options modal showing secure record sharing with doctor, caregiver, or family members plus delete option

Complete Genetic Record Management

Store, organize, and access all your genetic testing data with comprehensive tools for tracking variants, risk factors, and family health history.

Drug Response Tracking

Store medication metabolism information and genetic variants that affect drug effectiveness for safer prescribing decisions.

Disease Risk Monitoring

Track predispositions for hereditary conditions and connect genetic risks with your health conditions for preventive care planning.

Family Health History

Document genetic test results for family members to track inherited conditions and support genetic counseling discussions.

Carrier Screening Results

Store carrier status for hereditary conditions to support family planning decisions and reproductive health counseling.

Lab Result Integration

Correlate genetic variants with ongoing laboratory results to understand how your DNA influences biomarkers over time.

Updated Interpretations

Receive notifications when new research changes the clinical significance of your stored genetic variants.

Your Genetic Data is Protected

Military-grade encryption ensures your sensitive genomic information remains private and secure. Your DNA data is protected under HIPAA and genetic privacy regulations.

256-bit AES encryption for all genetic data
GINA-compliant genetic privacy protection
Controlled sharing with genetic counselors
Complete data ownership and export rights

Frequently Asked Questions

Common questions about storing genetic test results, protecting genomic data, and sharing findings with healthcare providers

CareClinic supports all major genetic test types including whole genome sequencing, exome sequencing, pharmacogenomic panels, carrier screening, ancestry testing, nutrigenomic profiles, cancer predisposition panels, and single gene tests. You can upload PDF reports from any laboratory or manually enter specific genetic variants and mutations.

Your genetic data is protected with 256-bit AES encryption for both storage and transmission. CareClinic is fully HIPAA-compliant and follows GINA genetic privacy principles. You control all sharing permissions, genetic data is never sold to third parties, and two-factor authentication provides additional security for accessing your genomic information.

Yes, CareClinic provides multiple secure sharing options. Generate comprehensive PDF reports with selected genetic variants, create temporary access links with expiration dates, or provide read-only access to specific test results. The app creates provider-friendly summaries highlighting clinically actionable variants relevant to treatment decisions.

Drug response genetic data helps identify medications requiring dose adjustments based on your genetic variants. Store test results showing drug metabolism information for antidepressants, blood thinners, pain medications, and cardiac drugs. This information supports safer prescribing decisions and personalized treatment planning with your healthcare provider.

Yes, create separate profiles for family members and build comprehensive family health trees. Document genetic test results for parents, siblings, children, and extended relatives to track inheritance patterns. This family genetic history helps identify hereditary conditions, supports cascade testing decisions, and provides valuable information for genetic counseling.

Yes, CareClinic provides notifications when new research affects your stored genetic variants. As medical understanding evolves, the app updates risk assessments and clinical significance ratings. You’ll receive alerts about newly discovered associations between your variants and health conditions, ensuring your genetic insights remain current with scientific advancement.

Yes, CareClinic accepts raw genetic data files from consumer testing services including 23andMe, AncestryDNA, MyHeritage DNA, and FamilyTreeDNA. The app processes VCF, CSV, and TXT formats containing genetic variant information. Once imported, your raw data is organized into clinically relevant categories and cross-referenced with medical databases.

Genetic risk scores identify conditions where you have elevated hereditary risk, enabling proactive health management. The app suggests appropriate screening schedules, lifestyle modifications, and preventive measures based on your genetic predispositions. Risk scores are presented with context about absolute versus relative risk to help make informed decisions about surveillance and prevention.

You maintain complete ownership of your genetic data. If you stop using CareClinic, export all genetic information in standard formats (PDF, CSV, JSON) for personal records or transfer to another platform. Upon account deletion request, your genetic data is permanently removed from CareClinic servers within 30 days, with confirmation provided once deletion is complete.